| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138028578-138028656 | Rare:17 | ||||
| chr3:138029546-138029906 | Common:3; Rare:63 | ||||
| chr3:138133269-138133377 | Rare:15 | ||||
| chr3:139352391-139352786 | Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:139354599-139354856 | Common:2; Rare:36 | ||||
| chr3:139355512-139355703 | Rare:41 | ||||
| chr3:139361275-139361475 | Rare:42 | ||||
| chr3:139362405-139362733 | Common:2; Rare:71 | ||||
| chr3:141406091-141406235 | Rare:20 | ||||
| chr3:141412940-141412968 | Rare:8 | ||||
| chr3:141429125-141429486 | Common:4; Rare:73 | ||||
| chr3:141660265-141660357 | Rare:29 | ||||
| chr3:141922877-141923144 | Common:3; Rare:50 | ||||
| chr3:146533599-146533783 | Common:3; Rare:24 | ||||
| chr3:149376936-149377038 | Rare:20 |